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GWAS Study

Novel exomic rare variants associated with venous thrombosis.

Deguchi H, Shukla M, Hayat M et al.

32232851 PubMed ID
GWAS Study Type
315 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DH
Deguchi H
SM
Shukla M
HM
Hayat M
TA
Torkamani A
ED
Elias DJ
GJ
Griffin JH
Chapter II

Abstract

Summary of the research findings

Exomic rare variant polymorphisms (c. 300 000) were analysed in the Scripps Venous Thrombosis (VTE) registry (subjects aged <55 years). Besides coagulation factor V (F5) single nucleotide polymorphisms (SNPs), family with sequence similarity 134, member B (FAM134B; rs78314670, Arg127Cys) and myosin heavy chain 8 (MYH8; rs111567318, Glu1838Ala) SNPs were associated with recurrent VTE (n = 34 cases) (false discovery rate-adjusted P < 0·05). FAM134B (rs78314670) was associated with low plasma levels of anticoagulant glucosylceramide. Analysis of 50 chr17p13.1 MYH rare SNPs (clustered skeletal myosin heavy chain genes) using collapsing methods was associated with recurrent VTE (P = 2·70 ×10-16 ). When intravenously injected, skeletal muscle myosin was pro-coagulant in a haemophilia mouse tail bleeding model. Thus, FAM134B and MYH genetic variants are plausibly linked to VTE risk.

104 European ancestry cases, 211 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

315
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

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